Director / Senior Director, Precision Diagnostics - Oncology

GSK

United States
Base: $189,750 to $316,250; bonus/equity: annual b...
Hybrid
8 years diagnostic development experience
2-3 years oncology diagnostic experience
Clinical trial design integration
GSK is seeking a Director/Senior Director for Precision Diagnostics in Oncology, responsible for leading diagnostic development efforts and cross-functional collaboration to improve patient outcomes. The ideal candidate will have extensive experience in diagnostic and biomarker strategy, particularly in oncology

Job Summary

  • The role involves implementing diagnostic development strategies that align with oncology development needs to treat the right patient with the right medicine.
  • Candidates must have at least 8 years of experience in diagnostic development and 2 to 3 years specifically in oncology diagnostic development.
  • The position offers a competitive annual base salary ranging from $189,750 to $316,250 depending on location, along with bonus eligibility and comprehensive benefits.

Matching Summary

Match Score: 85

GSK is seeking a Director/Senior Director for Precision Diagnostics in Oncology, responsible for leading diagnostic development efforts and cross-functional collaboration to improve patient outcomes. The ideal candidate will have extensive experience in diagnostic and biomarker strategy, particularly in oncology.

Salary

Base: $189,750 to $316,250; Bonus/Equity: Annual bonus and share-based long term incentive program; Benefits: Health care, retirement, paid holidays, vacation, and parental leave

Skills & Requirements

Must-have

  • 8 years diagnostic development experience
  • 2-3 years oncology diagnostic experience
  • Clinical trial design integration
  • FDA and EU medical device regulations
  • Cross-functional project management
  • Biomarker strategy and assay validation

Nice-to-have

  • Advanced degree in life sciences
  • Next-generation sequencing (NGS) experience
  • Regulatory submission interactions
  • Commercial team partnership experience
  • Laboratory accreditation standards knowledge
  • Curiosity and humility mindset

Key Requirements

  • Bachelor's degree in life sciences or related field
  • Master's, PhD, or MD preferred
  • Knowledge of ISO13485 and GMP manufacturing
  • Experience with human biological specimen management
  • Proven ability to manage budgets and timelines

Work Rights

Not specified

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